-
1
-
-
0000610199
-
-
(Chemische Verwertungsgesellschaft, mbH Oberhausen) German Patent DE 849,548, 1938/1952; U.S. Patent 2,317,066, 1943
-
Roelen, O. (Chemische Verwertungsgesellschaft, mbH Oberhausen) German Patent DE 849,548, 1938/1952; U.S. Patent 2,317,066, 1943; Chem. Abstr. 1944, 38, 550.
-
(1944)
Chem. Abstr.
, vol.38
, pp. 550
-
-
Roelen, O.1
-
3
-
-
0026418434
-
The atom economy - A search for synthetic efficiency
-
Trost, B. M. The Atom Economy - A Search for Synthetic Efficiency. Science 1991, 254, 1471-1477; Atom Economy - A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way. Angew. Chem., Int. Ed. Engl. 1995, 34, 259-281.
-
(1991)
Science
, vol.254
, pp. 1471-1477
-
-
Trost, B.M.1
-
4
-
-
33750309194
-
Atom economy - A challenge for organic synthesis: Homogeneous catalysis leads the way
-
Trost, B. M. The Atom Economy - A Search for Synthetic Efficiency. Science 1991, 254, 1471-1477; Atom Economy - A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way. Angew. Chem., Int. Ed. Engl. 1995, 34, 259-281.
-
(1995)
Angew. Chem., Int. Ed. Engl.
, vol.34
, pp. 259-281
-
-
-
5
-
-
0035157151
-
Recent advances on chemo-regio- and stereoselective hydroformylation
-
Breit, B.; Seiche, W. Recent Advances on Chemo-Regio- and Stereoselective Hydroformylation. Synthesis 2001, 1-36.
-
(2001)
Synthesis
, pp. 1-36
-
-
Breit, B.1
Seiche, W.2
-
6
-
-
37049124551
-
Hydroformylation of alkenes by use of rhodium complex catalysts
-
Evans, D. A.; Osborn, J. A.; Wilkinson, G. Hydroformylation of Alkenes by Use of Rhodium Complex Catalysts. J. Chem. Soc. A 1968, 3133-3142. Brown, C. K.; Wilkinson, G. Homogeneous Hydroformylation of Alkenes with Hydridocarbonyltris-(triphenylphosphine)rhodium(I) as Catalyst. J. Chem. Soc. A 1970, 17, 2753-2764. Wilkinson, G. Homogeneous Hydrogenation and Hydroformylation of Olefins by Rhodium Triphenylphosphine Catalysts. Bull. Soc. Chim. Fr. 1968, 5055-5058. Osborn, J. A.; Jardine, F. H.; Young, J. F.; Wilkinson, G. The Preparation and Properties of Tris(triphenylphosphine)halogeno-rhodium(I) and Some Reactions thereof including Catalytic Homogeneous Hydrogenation of Olefins and Acetylenes and their Derivatives. J. Chem. Soc. A 1966, 1711-1732.
-
(1968)
J. Chem. Soc. A
, pp. 3133-3142
-
-
Evans, D.A.1
Osborn, J.A.2
Wilkinson, G.3
-
7
-
-
37049125199
-
Homogeneous hydroformylation of alkenes with hydridocarbonyltris-(triphenylphosphine)rhodium(I) as catalyst
-
Evans, D. A.; Osborn, J. A.; Wilkinson, G. Hydroformylation of Alkenes by Use of Rhodium Complex Catalysts. J. Chem. Soc. A 1968, 3133-3142. Brown, C. K.; Wilkinson, G. Homogeneous Hydroformylation of Alkenes with Hydridocarbonyltris-(triphenylphosphine)rhodium(I) as Catalyst. J. Chem. Soc. A 1970, 17, 2753-2764. Wilkinson, G. Homogeneous Hydrogenation and Hydroformylation of Olefins by Rhodium Triphenylphosphine Catalysts. Bull. Soc. Chim. Fr. 1968, 5055-5058. Osborn, J. A.; Jardine, F. H.; Young, J. F.; Wilkinson, G. The Preparation and Properties of Tris(triphenylphosphine)halogeno-rhodium(I) and Some Reactions thereof including Catalytic Homogeneous Hydrogenation of Olefins and Acetylenes and their Derivatives. J. Chem. Soc. A 1966, 1711-1732.
-
(1970)
J. Chem. Soc. A
, vol.17
, pp. 2753-2764
-
-
Brown, C.K.1
Wilkinson, G.2
-
8
-
-
0002980921
-
Homogeneous hydrogenation and hydroformylation of olefins by rhodium triphenylphosphine catalysts
-
Evans, D. A.; Osborn, J. A.; Wilkinson, G. Hydroformylation of Alkenes by Use of Rhodium Complex Catalysts. J. Chem. Soc. A 1968, 3133-3142. Brown, C. K.; Wilkinson, G. Homogeneous Hydroformylation of Alkenes with Hydridocarbonyltris-(triphenylphosphine)rhodium(I) as Catalyst. J. Chem. Soc. A 1970, 17, 2753-2764. Wilkinson, G. Homogeneous Hydrogenation and Hydroformylation of Olefins by Rhodium Triphenylphosphine Catalysts. Bull. Soc. Chim. Fr. 1968, 5055-5058. Osborn, J. A.; Jardine, F. H.; Young, J. F.; Wilkinson, G. The Preparation and Properties of Tris(triphenylphosphine)halogeno-rhodium(I) and Some Reactions thereof including Catalytic Homogeneous Hydrogenation of Olefins and Acetylenes and their Derivatives. J. Chem. Soc. A 1966, 1711-1732.
-
(1968)
Bull. Soc. Chim. Fr.
, pp. 5055-5058
-
-
Wilkinson, G.1
-
9
-
-
37049133322
-
The preparation and properties of tris(triphenylphosphine)halogeno-rhodium(I) and some reactions thereof including catalytic homogeneous hydrogenation of olefins and acetylenes and their derivatives
-
Evans, D. A.; Osborn, J. A.; Wilkinson, G. Hydroformylation of Alkenes by Use of Rhodium Complex Catalysts. J. Chem. Soc. A 1968, 3133-3142. Brown, C. K.; Wilkinson, G. Homogeneous Hydroformylation of Alkenes with Hydridocarbonyltris-(triphenylphosphine)rhodium(I) as Catalyst. J. Chem. Soc. A 1970, 17, 2753-2764. Wilkinson, G. Homogeneous Hydrogenation and Hydroformylation of Olefins by Rhodium Triphenylphosphine Catalysts. Bull. Soc. Chim. Fr. 1968, 5055-5058. Osborn, J. A.; Jardine, F. H.; Young, J. F.; Wilkinson, G. The Preparation and Properties of Tris(triphenylphosphine)halogeno-rhodium(I) and Some Reactions thereof including Catalytic Homogeneous Hydrogenation of Olefins and Acetylenes and their Derivatives. J. Chem. Soc. A 1966, 1711-1732.
-
(1966)
J. Chem. Soc. A
, pp. 1711-1732
-
-
Osborn, J.A.1
Jardine, F.H.2
Young, J.F.3
Wilkinson, G.4
-
10
-
-
0000965498
-
-
U.S. Patent 4,694,109, 1987
-
Devon, T. J.; Phillips, G. W.; Puckette, T. A.; Stavinoha, J. L.; Vanderbilt, J. J. U.S. Patent 4,694,109, 1987; Chem. Abstr. 1988, 108, 7890.
-
(1988)
Chem. Abstr.
, vol.108
, pp. 7890
-
-
Devon, T.J.1
Phillips, G.W.2
Puckette, T.A.3
Stavinoha, J.L.4
Vanderbilt, J.J.5
-
11
-
-
85005607967
-
The natural bite angle of chelating diphosphines
-
Casey, C. P.; Whiteker, G. T. The natural bite angle of chelating diphosphines. Isr. J. Chem. 1990, 30, 299-304.
-
(1990)
Isr. J. Chem.
, vol.30
, pp. 299-304
-
-
Casey, C.P.1
Whiteker, G.T.2
-
12
-
-
11944256836
-
Diphosphines with natural bite angles near 120.degree. Increase selectivity for n-aldehyde formation in rhodium-catalyzed hydroformylation
-
Casey, C. P.; Whiteker, G. T.; Melville, M. G.; Petrovich, L. M.; Gavey, J. A.; Powell, D. R. Diphosphines with natural bite angles near 120.degree. Increase selectivity for n-aldehyde formation in rhodium-catalyzed hydroformylation. J. Am. Chem. Soc. 1992, 114, 5535-5543.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 5535-5543
-
-
Casey, C.P.1
Whiteker, G.T.2
Melville, M.G.3
Petrovich, L.M.4
Gavey, J.A.5
Powell, D.R.6
-
13
-
-
84921186420
-
-
(UCC) U.S. Patent 4,769,498, 1988
-
Billig, E.; Abatjoglou, A. G.; Bryant, D. R. (UCC) U.S. Patent 4,769,498, 1988; Chem. Abstr. 1989, 111, 117 287. Cunny, G. D.; Buchwald, S. L. Practical, high-yield, regioselective, rhodiumcatalyzed hydroformylation of functionalized.alpha.-olefins. J. Am. Chem. Soc. 1993, 115, 2066-2068.
-
(1989)
Chem. Abstr.
, vol.111
, pp. 117-287
-
-
Billig, E.1
Abatjoglou, A.G.2
Bryant, D.R.3
-
14
-
-
84921186420
-
Practical, high-yield, regioselective, rhodiumcatalyzed hydroformylation of functionalized.alpha.-olefins
-
Billig, E.; Abatjoglou, A. G.; Bryant, D. R. (UCC) U.S. Patent 4,769,498, 1988; Chem. Abstr. 1989, 111, 117 287. Cunny, G. D.; Buchwald, S. L. Practical, high-yield, regioselective, rhodiumcatalyzed hydroformylation of functionalized.alpha.-olefins. J. Am. Chem. Soc. 1993, 115, 2066-2068.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 2066-2068
-
-
Cunny, G.D.1
Buchwald, S.L.2
-
15
-
-
0001029926
-
New diphosphine ligands based on heterocyclic aromatics inducing very high regioselectivity in rhodium-catalyzed hydroformylation: Effect of the bite angle
-
Kranenburg, M.; van der Burgt, Y. E. M.; Kamer, P. C. J.; van Leeuwen, P. W. N. M.; Goubitz, K.; Fraanje, J. New Diphosphine Ligands Based on Heterocyclic Aromatics Inducing Very High Regioselectivity in Rhodium-Catalyzed Hydroformylation: Effect of the Bite Angle. Organometallics 1995, 14, 3081-3089. Kamer C. J. P.; van Leeuwen, P. W. N. M.; Reek, J. N. H. Wide Bite Angle Diphosphines: Xantphos Ligands in Transition Metal Complexes and Catalysis. Acc. Chem. Res. 2001, 34, 895-904.
-
(1995)
Organometallics
, vol.14
, pp. 3081-3089
-
-
Kranenburg, M.1
Van der Burgt, Y.E.M.2
Kamer, P.C.J.3
Van Leeuwen, P.W.N.M.4
Goubitz, K.5
Fraanje, J.6
-
16
-
-
0035200787
-
Wide bite angle diphosphines: Xantphos ligands in transition metal complexes and catalysis
-
Kranenburg, M.; van der Burgt, Y. E. M.; Kamer, P. C. J.; van Leeuwen, P. W. N. M.; Goubitz, K.; Fraanje, J. New Diphosphine Ligands Based on Heterocyclic Aromatics Inducing Very High Regioselectivity in Rhodium-Catalyzed Hydroformylation: Effect of the Bite Angle. Organometallics 1995, 14, 3081-3089. Kamer C. J. P.; van Leeuwen, P. W. N. M.; Reek, J. N. H. Wide Bite Angle Diphosphines: Xantphos Ligands in Transition Metal Complexes and Catalysis. Acc. Chem. Res. 2001, 34, 895-904.
-
(2001)
Acc. Chem. Res.
, vol.34
, pp. 895-904
-
-
Kamer, C.J.P.1
Van Leeuwen, P.W.N.M.2
Reek, J.N.H.3
-
17
-
-
0000613575
-
Asymmetric hydroformylation
-
Agbossou, F.; Carpentier, J. F.; Mortreux, A. Asymmetric Hydroformylation. Chem. Rev. 1995, 95, 2485-2506.
-
(1995)
Chem. Rev.
, vol.95
, pp. 2485-2506
-
-
Agbossou, F.1
Carpentier, J.F.2
Mortreux, A.3
-
18
-
-
85013461641
-
Highly enantioselective hydroformylation of olefins catalyzed by new phosphine phosphite-rhodium(I) complexes
-
Sakai, N.; Mano, S.; Nozaki, K.; Takaya, H. Highly enantioselective hydroformylation of olefins catalyzed by new phosphine phosphite-rhodium(I) complexes. J. Am. Chem. Soc. 1993, 115, 7033. Nozaki, K.; Ojima, I. Asymmetric Carbonylations. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; Wiley-VCH: New York, 2000; Chapter 7.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 7033
-
-
Sakai, N.1
Mano, S.2
Nozaki, K.3
Takaya, H.4
-
19
-
-
85013461641
-
Asymmetric carbonylations
-
Ojima, I., Ed.; Wiley-VCH: New York; Chapter 7
-
Sakai, N.; Mano, S.; Nozaki, K.; Takaya, H. Highly enantioselective hydroformylation of olefins catalyzed by new phosphine phosphite-rhodium(I) complexes. J. Am. Chem. Soc. 1993, 115, 7033. Nozaki, K.; Ojima, I. Asymmetric Carbonylations. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; Wiley-VCH: New York, 2000; Chapter 7.
-
(2000)
Catalytic Asymmetric Synthesis
-
-
Nozaki, K.1
Ojima, I.2
-
20
-
-
0001475165
-
Synthese von zwischenprodukten durch rhodiumkatalysierte hydroformylierung
-
Siegel, H.; Himmele W. Synthese von Zwischenprodukten durch rhodiumkatalysierte Hydroformylierung. Angew. Chem. 1980, 92, 182-187; Synthesis of intermediate products by rhodiumcatalyzed hydroformylation. Angew. Chem., Int. Ed. Engl. 1980, 19, 178-183.
-
(1980)
Angew. Chem.
, vol.92
, pp. 182-187
-
-
Siegel, H.1
Himmele, W.2
-
21
-
-
84985560802
-
Synthesis of intermediate products by rhodiumcatalyzed hydroformylation
-
Siegel, H.; Himmele W. Synthese von Zwischenprodukten durch rhodiumkatalysierte Hydroformylierung. Angew. Chem. 1980, 92, 182-187; Synthesis of intermediate products by rhodiumcatalyzed hydroformylation. Angew. Chem., Int. Ed. Engl. 1980, 19, 178-183.
-
(1980)
Angew. Chem., Int. Ed. Engl.
, vol.19
, pp. 178-183
-
-
-
22
-
-
0035898365
-
Phosphabenzenes as monodentate π-acceptor ligands for rhodium-catalyzed hydroformylation
-
Breit, B.; Winde, R.; Mackewitz, T.; Paciello, R.; Harms, K. Phosphabenzenes as Monodentate π-Acceptor Ligands for Rhodium-Catalyzed Hydroformylation. Chem. Eur. J. 2001, 7, 3106-3121.
-
(2001)
Chem. Eur. J.
, vol.7
, pp. 3106-3121
-
-
Breit, B.1
Winde, R.2
Mackewitz, T.3
Paciello, R.4
Harms, K.5
-
23
-
-
0025113889
-
Total synthesis of (+)-phyllanthocin. Introduction of intramolecular hydroformylation for complex molecule functionalization
-
Burke, S. D.; Cobb, J. E.; Takeuchi, K. Total synthesis of (+)-phyllanthocin. Introduction of intramolecular hydroformylation for complex molecule functionalization. J. Org. Chem. 1990, 55, 2138-2151.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 2138-2151
-
-
Burke, S.D.1
Cobb, J.E.2
Takeuchi, K.3
-
24
-
-
84970564851
-
The stereochemistry of organometallic compounds. XXXVIII* regio- and stereo-control in the rhodium-catalysed hydroformylation of some alkenyl phosphites
-
Jackson, W. R.; Moffat, M. R.; Perlmutter, P.; Tasdelen, E. E. The Stereochemistry of Organometallic Compounds. XXXVIII* Regio- and Stereo-control in the Rhodium-Catalysed Hydroformylation of Some Alkenyl Phosphites. Aust. J. Chem. 1992, 45, 823-834.
-
(1992)
Aust. J. Chem.
, vol.45
, pp. 823-834
-
-
Jackson, W.R.1
Moffat, M.R.2
Perlmutter, P.3
Tasdelen, E.E.4
-
25
-
-
0030590401
-
Diastereoselective hydroformylation of certain protected allylic alcohols
-
Doi, T.; Komatsu, H.; Yamamoto, K. Diastereoselective Hydroformylation of Certain Protected Allylic Alcohols. Tetrahedron Lett. 1996, 37, 6877-6880.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 6877-6880
-
-
Doi, T.1
Komatsu, H.2
Yamamoto, K.3
-
26
-
-
0000458209
-
Substrate-directable reactions
-
Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Substrate-Directable Reactions. Chem. Rev. 1993, 93, 1307-1370. Brown, J. M. Intramolekular gesteuerte katalytische Hydrierungen in homogener Phase. Angew. Chem. 1987, 99, 169-182; Directed Homogeneous Hydrogenation. Angew. Chem., Int. Ed. Engl. 1987, 26, 190-203.
-
(1993)
Chem. Rev.
, vol.93
, pp. 1307-1370
-
-
Hoveyda, A.H.1
Evans, D.A.2
Fu, G.C.3
-
27
-
-
0000458209
-
Intramolekular gesteuerte katalytische hydrierungen in homogener phase
-
Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Substrate-Directable Reactions. Chem. Rev. 1993, 93, 1307-1370. Brown, J. M. Intramolekular gesteuerte katalytische Hydrierungen in homogener Phase. Angew. Chem. 1987, 99, 169-182; Directed Homogeneous Hydrogenation. Angew. Chem., Int. Ed. Engl. 1987, 26, 190-203.
-
(1987)
Angew. Chem.
, vol.99
, pp. 169-182
-
-
Brown, J.M.1
-
28
-
-
84985560333
-
Directed homogeneous hydrogenation
-
Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Substrate-Directable Reactions. Chem. Rev. 1993, 93, 1307-1370. Brown, J. M. Intramolekular gesteuerte katalytische Hydrierungen in homogener Phase. Angew. Chem. 1987, 99, 169-182; Directed Homogeneous Hydrogenation. Angew. Chem., Int. Ed. Engl. 1987, 26, 190-203.
-
(1987)
Angew. Chem., Int. Ed. Engl.
, vol.26
, pp. 190-203
-
-
-
29
-
-
0000680768
-
Diastereoselective hydroformylation of methallylic alcohols
-
Breit, B. Diastereoselective Hydroformylation of Methallylic Alcohols. Angew. Chem. 1996, 108, 3021-3023; Angew. Chem., Int. Ed. Engl. 1996, 35, 2835-2837.
-
(1996)
Angew. Chem.
, vol.108
, pp. 3021-3023
-
-
Breit, B.1
-
30
-
-
0030484567
-
-
Breit, B. Diastereoselective Hydroformylation of Methallylic Alcohols. Angew. Chem. 1996, 108, 3021-3023; Angew. Chem., Int. Ed. Engl. 1996, 35, 2835-2837.
-
(1996)
Angew. Chem., Int. Ed. Engl.
, vol.35
, pp. 2835-2837
-
-
-
31
-
-
0003719460
-
Substrate-directed diastereoselective hydroformylation of methallylic alcohols-development of an efficient catalyst-directing group for rhodium-catalyzed hydroformylation
-
Breit, B. Substrate-Directed Diastereoselective Hydroformylation of Methallylic Alcohols-Development of an Efficient Catalyst-Directing Group for Rhodium-Catalyzed Hydroformylation. Liebigs Ann./Recueil 1997, 1841-1851.
-
(1997)
Liebigs Ann./Recueil
, pp. 1841-1851
-
-
Breit, B.1
-
32
-
-
0002177913
-
Asymmetric allylic alkylation
-
Ojima, I., Ed.; Wiley-VCH: New York, Chapter 8E
-
Ortho-diphenylbenzoic acid is also an integral part of the Trost type ligands for the enantioselective palladium-catalyzed allylic substitution, see: Trost, B. M.; Chulbom L. Asymmetric Allylic Alkylation. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; Wiley-VCH: New York, 2000, Chapter 8E.
-
(2000)
Catalytic Asymmetric Synthesis
-
-
Trost, B.M.1
Chulbom, L.2
-
33
-
-
0344640634
-
-
Unpublished results from these laboratories
-
Breit, B.; Zahn, S. K. Unpublished results from these laboratories, 2001.
-
(2001)
-
-
Breit, B.1
Zahn, S.K.2
-
34
-
-
0037455326
-
Diastereoselective hydroformylation of 2-substituted allylic-o-DPPB-esters - On the origin of 1,2-asymmetric induction
-
in press
-
Breit, B.; Heckmann, G.; Zahn, S. K. Diastereoselective Hydroformylation of 2-Substituted Allylic-o-DPPB-Esters - On the Origin of 1,2-Asymmetric Induction. Chem. Eur. J. 2003, 9, in press.
-
(2003)
Chem. Eur. J.
, vol.9
-
-
Breit, B.1
Heckmann, G.2
Zahn, S.K.3
-
35
-
-
0032820019
-
Substrate-directed diastereoselective hydroformylation: Key step for the assembly of polypropionate subunits
-
Breit, B.; Dauber, M.; Harms, K. Substrate-Directed Diastereoselective Hydroformylation: Key step for the Assembly of Polypropionate Subunits, Chem. Eur. J. 1999, 5, 2819-2827.
-
(1999)
Chem. Eur. J.
, vol.5
, pp. 2819-2827
-
-
Breit, B.1
Dauber, M.2
Harms, K.3
-
36
-
-
84985611207
-
Stereoselective syntheses of building blocks with three consecutive stereogenic centers: Important precursors of polyketide natural products
-
Hoffmann, R. W. Stereoselective Syntheses of Building Blocks with Three Consecutive Stereogenic Centers: Important Precursors of Polyketide Natural Products. Angew. Chem., Int. Ed. Engl. 1987, 26, 489-503.
-
(1987)
Angew. Chem., Int. Ed. Engl.
, vol.26
, pp. 489-503
-
-
Hoffmann, R.W.1
-
37
-
-
0035854318
-
Stereoselective hydroformylation: Key step for the assembly of polypropionate subunits
-
Breit, B.; Zahn, S. K. Stereoselective Hydroformylation: Key Step for the Assembly of Polypropionate Subunits. J. Org. Chem. 2001, 66, 4870-4877.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 4870-4877
-
-
Breit, B.1
Zahn, S.K.2
-
38
-
-
0032473817
-
Diastereoselective hydroformylation of acyclic olefins: Efficient construction of an all-anti stereotriade building block for polyketide synthesis
-
Breit, B.; Zahn, S. K. Diastereoselective hydroformylation of acyclic olefins: efficient construction of an all-anti stereotriade building block for polyketide synthesis. Tetrahedron Lett. 1998, 39, 1901-1904.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 1901-1904
-
-
Breit, B.1
Zahn, S.K.2
-
39
-
-
0001449130
-
Highly stereoselective hydroformylation of olefins possessing chiral sugartemplates
-
Takahashi, T.; Ebata, S.; Yamada, H. Highly stereoselective hydroformylation of olefins possessing chiral sugartemplates. Synlett. 1998, 381-382.
-
(1998)
Synlett
, pp. 381-382
-
-
Takahashi, T.1
Ebata, S.2
Yamada, H.3
-
40
-
-
0035929981
-
Highly regioselective and diastereoselective directed hydroformylation of allylic ethers: A new approach to propionate aldol synthesis
-
Krauss, I. J.; Wang, C. C.-Y.; Leighton, J. L. Highly Regioselective and Diastereoselective Directed Hydroformylation of Allylic Ethers: A New Approach to Propionate Aldol Synthesis. J. Am. Chem. Soc. 2001, 123, 11514-11515.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 11514-11515
-
-
Krauss, I.J.1
Wang, C.C.-Y.2
Leighton, J.L.3
-
41
-
-
0000287486
-
Substrate directed diastereoselective hydroformylation of acyclic homomethallylic alcohols
-
Breit, B. Substrate directed diastereoselective hydroformylation of acyclic homomethallylic alcohols. J. Chem. Soc., Chem. Commun. 1997, 591-592.
-
(1997)
J. Chem. Soc., Chem. Commun.
, pp. 591-592
-
-
Breit, B.1
-
42
-
-
2742537764
-
1,3-Asymmetric induction in stereoselective rhodium-catalyzed hydroformylation of homomethallylic alcohols
-
Breit, B. 1,3-Asymmetric Induction in Stereoselective Rhodium-Catalyzed Hydroformylation of Homomethallylic Alcohols. Eur. J. Org. Chem. 1998, 3, 1123-1134.
-
(1998)
Eur. J. Org. Chem.
, vol.3
, pp. 1123-1134
-
-
Breit, B.1
-
43
-
-
0030726113
-
Highly diastereoselective rhodium-catalyzed hydroformylation of enol ethers: A carbonylation-based approach to catalytic aldol synthesis
-
Leighton, J. L.; O'Neil, D. N. Highly Diastereoselective Rhodium-Catalyzed Hydroformylation of Enol Ethers: A Carbonylation-Based Approach to Catalytic Aldol Synthesis. J. Am. Chem. Soc. 1997, 119, 11118-11119.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 11118-11119
-
-
Leighton, J.L.1
O'Neil, D.N.2
-
44
-
-
0000777791
-
Tandem reaction sequences under hydroformylation conditions: New synthetic applications of transition metal catalysis
-
Eilbracht, P.; Bärfacker, L.; Buss, C.; Hollmann, C.; Kitsos-Rzychon, B. E.; Kranemann, C. L.; Rische, T.; Roggenbuck, R.; Schmidt. A. Tandem Reaction Sequences under Hydroformylation Conditions: New Synthetic Applications of Transition Metal Catalysis. Chem. Rev. 1999, 99, 3329-3366.
-
(1999)
Chem. Rev.
, vol.99
, pp. 3329-3366
-
-
Eilbracht, P.1
Bärfacker, L.2
Buss, C.3
Hollmann, C.4
Kitsos-Rzychon, B.E.5
Kranemann, C.L.6
Rische, T.7
Roggenbuck, R.8
Schmidt, A.9
-
45
-
-
84975921727
-
-
(IG Farben), DRP, a. I. 74,946, 1943
-
Reppe, W. (IG Farben), DRP, a. I. 74,946, 1943; Reppe, W.; Kindler, W. Synthese mit Metallcarbonylwasserstoffen. Liebigs Ann. Chem. 1953, 582, 133-161.
-
-
-
Reppe, W.1
-
46
-
-
84975921727
-
Synthese mit metallcarbonylwasserstoffen
-
Reppe, W. (IG Farben), DRP, a. I. 74,946, 1943; Reppe, W.; Kindler, W. Synthese mit Metallcarbonylwasserstoffen. Liebigs Ann. Chem. 1953, 582, 133-161.
-
(1953)
Liebigs Ann. Chem.
, vol.582
, pp. 133-161
-
-
Reppe, W.1
Kindler, W.2
-
47
-
-
0032537696
-
Substrate-directed diastereoselective hydroaminomethylation of methallylic alcohols
-
B. Breit Substrate-Directed Diastereoselective Hydroaminomethylation of Methallylic Alcohols. Tetrahedron Lett. 1998, 39, 5163-5166.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 5163-5166
-
-
Breit, B.1
-
48
-
-
0034678104
-
Tandem hydroformylation/aldol addition of silyl enol ethers bearing remote olefinic functionalities
-
Hollmann, C.; Eilbracht, P. Tandem Hydroformylation/Aldol Addition of Silyl Enol Ethers Bearing Remote Olefinic Functionalities. Tetrahedron 2000, 56, 1685-1692.
-
(2000)
Tetrahedron
, vol.56
, pp. 1685-1692
-
-
Hollmann, C.1
Eilbracht, P.2
-
49
-
-
0342614249
-
Domino-hydroformylation-allylboration-hydroformylation for the synthesis of trans-2-alkylpiperidin-3-ols
-
Hoffmann, R. W.; Brückner, D.; Gerusz, V. J. Domino-hydroformylation-allylboration-hydroformylation for the synthesis of trans-2-alkylpiperidin-3-ols. Heterocycles 2000, 52, 121-124.
-
(2000)
Heterocycles
, vol.52
, pp. 121-124
-
-
Hoffmann, R.W.1
Brückner, D.2
Gerusz, V.J.3
-
50
-
-
0001615148
-
Domino hydroformylation wittig reactions
-
Breit, B.; Zahn, S. K. Domino Hydroformylation Wittig Reactions. Angew. Chem. 1999, 111, 1022-1024; Angew. Chem., Int. Ed. Engl. 1999, 38, 969-971.
-
(1999)
Angew. Chem.
, vol.111
, pp. 1022-1024
-
-
Breit, B.1
Zahn, S.K.2
-
51
-
-
0033119121
-
-
Breit, B.; Zahn, S. K. Domino Hydroformylation Wittig Reactions. Angew. Chem. 1999, 111, 1022-1024; Angew. Chem., Int. Ed. Engl. 1999, 38, 969-971.
-
(1999)
Angew. Chem., Int. Ed. Engl.
, vol.38
, pp. 969-971
-
-
-
52
-
-
0000020751
-
Domino hydroformylation-knoevenagel-hydrogenation reactions
-
Breit, B.; Zahn, S. K. Domino Hydroformylation-Knoevenagel-Hydrogenation Reactions. Angew. Chem. 2001, 113, 1964-1967; Angew. Chem., Int. Ed. 2001, 40, 1910-1913.
-
(2001)
Angew. Chem.
, vol.113
, pp. 1964-1967
-
-
Breit, B.1
Zahn, S.K.2
-
53
-
-
0035906868
-
-
Breit, B.; Zahn, S. K. Domino Hydroformylation-Knoevenagel-Hydrogenation Reactions. Angew. Chem. 2001, 113, 1964-1967; Angew. Chem., Int. Ed. 2001, 40, 1910-1913.
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 1910-1913
-
-
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